Package 71993-308-90

Brand: fenoprofen calcium

Generic: fenoprofen calcium
NDC Package

Package Facts

Identity

Package NDC 71993-308-90
Digits Only 7199330890
Product NDC 71993-308
Description

90 CAPSULE in 1 BOTTLE (71993-308-90)

Marketing

Marketing Status
Marketed Since 2024-03-26
Brand fenoprofen calcium
Generic fenoprofen calcium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "14a4aa5b-30ff-8ad7-e063-6294a90a889e", "openfda": {"upc": ["0371993308900"], "unii": ["0X2CW1QABJ"], "rxcui": ["858116"], "spl_set_id": ["3daa336f-2acf-4109-a360-b1d30b192d41"], "manufacturer_name": ["Atland Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71993-308-90)", "package_ndc": "71993-308-90", "marketing_start_date": "20240326"}], "brand_name": "FENOPROFEN CALCIUM", "product_id": "71993-308_14a4aa5b-30ff-8ad7-e063-6294a90a889e", "dosage_form": "CAPSULE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71993-308", "generic_name": "FENOPROFEN CALCIUM", "labeler_name": "Atland Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FENOPROFEN CALCIUM", "active_ingredients": [{"name": "FENOPROFEN CALCIUM", "strength": "400 mg/1"}], "application_number": "ANDA214475", "marketing_category": "ANDA", "marketing_start_date": "20240326", "listing_expiration_date": "20261231"}